Work Setup: On-site
Schedule: Part-time, 24 hours per week
About IQVIA
IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services. We partner with leading pharmaceutical, biotechnology, and medical device companies to advance healthcare and improve patient outcomes. By combining deep scientific expertise with innovative technologies, IQVIA delivers the high‑quality evidence needed to drive clinical development forward.
About the Role
IQVIA is seeking a Spanish Bilingual Clinical Research Coordinator (CRC) to support clinical research studies conducted under the supervision of a Principal Investigator. This hands‑on role is ideal for a detail‑oriented professional with prior coordinating experience who is comfortable working directly with patients, managing study data, and ensuring strict adherence to study protocols and Good Clinical Practice (GCP).
The CRC plays a critical role in the day‑to‑day execution of clinical trials, patient safety, and data integrity.
Key Responsibilities
Conduct and support participant visits, including clinical procedures such as ECGs, vital signs, and biological sample collection
Coordinate study activities in compliance with protocols, GCP, and regulatory requirements
Prepare study materials, organize equipment, and support logistical planning for study visits
Assist with patient recruitment, screening, consent, and visit coordination
Perform accurate electronic data capture (EDC) entry, query resolution, and source documentation
Maintain investigational product (IP) accountability, including reconciliation and documentation
Conduct chart reviews to support eligibility determination and data verification
Collaborate closely with investigators, sponsors, and monitors to resolve study issues and maintain data quality
Serve as a patient advocate, ensuring participant safety, comfort, and confidentiality
Uphold Health & Safety and quality standards across all study activities
Qualifications & Experience
Bachelor’s degree preferred, or an equivalent combination of education and relevant experience
Minimum of 1+ year of hands‑on clinical research coordinating experience
Demonstrated experience with:
Patient-facing study visits
EDC data entry and query resolution
Patient recruitment and screening
Investigational Product (IP) accountability
Source document and chart review
Working knowledge of clinical trials, GCP, and medical terminology
Strong attention to detail with the ability to manage multiple priorities
Ability to build effective working relationships with study teams and participants
Fluency in Spanish required (spoken and written); English proficiency preferred
Comfortable working on-site and independently within a structured research environment
Additional Information
This is an on-site, part-time position (24 hours/week)
Not eligible for visa sponsorshi
#LI-CES and #LI-DNP #LI-HCP #remote
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
The potential base pay range for this role, when annualized, is $41,000.00 - $118,600.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.